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The American Journal of Geriatric Psychiatry, ISSN 1064-7481, 03/2019, Volume 27, Issue 3, pp. S48 - S48
Journal Article
The American Journal of Geriatric Psychiatry, ISSN 1064-7481, 03/2019, Volume 27, Issue 3, p. S48
Journal Article
Academic psychiatry : the journal of the American Association of Directors of Psychiatric Residency Training and the Association for Academic Psychiatry, ISSN 1042-9670, 06/2019
The authors describe a novel curricular intervention that enhances first- and second-year psychiatry residents' geriatric psychiatry knowledge while preparing... 
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 02/2012, Volume 90, Issue 2, p. 331
Complete congenital stationary night blindness (cCSNB) is a clinically and genetically heterogeneous group of retinal disorders characterized by nonprogressive... 
Proteins | Genetic disorders | Rodents | Blindness | Mutation | Gene expression | Cells
Journal Article
Nucleic Acids Research, ISSN 0305-1048, 1989, Volume 17, Issue 1, pp. 107 - 117
Journal Article
Allemagne d'aujourd'hui, ISSN 0002-5712, 2019, Volume N° 229, Issue 3, p. 135
Journal Article
by Shitara, Kohei and Özgüroğlu, Mustafa and Bang, Yung-Jue and Di Bartolomeo, Maria and Mandalà, Mario and Ryu, Min-Hee and Fornaro, Lorenzo and Olesiński, Tomasz and Caglevic, Christian and Chung, Hyun C and Chung, Hyun Cheol and Muro, Kei and Goekkurt, Eray and Mansoor, Wasat and McDermott, Raymond S and Shacham-Shmueli, Einat and Chen, Xinqun and Chen, Jen-Shi and Mayo, Carlos and Kang, S Peter and Ohtsu, Atsushi and Fuchs, Charles S and Lerzo, Guillermo and O'Connor, Juan Manuel and Mendez, Guillermo Ariel and Lynam, James and Tebbutt, Niall and Wong, Mark and Strickland, Andrew and Karapetis, Chris and Goldstein, David and Vasey, Paul and Van Laethem, Jean-Luc and Van Cutsem, Eric and Berry, Scott and Vincent, Mark and Muller, Bettina and Rey, Felipe and Zambrano, Angela and Guerra, Joaquin and Krogh, Merete and Baeksgaard, Lene and Yilmaz, Mette and Elme, Anneli and Magi, Andrus and Auvinen, Paivi and Alanko, Tuomo and Moehler, Markus and Kunzmann, Volker and Seufferlein, Thomas and Thuss-Patience, Peter and Hoehler, Thomas and Haag, Georg and Al-Batran, Salah-Eddin and Castro, Hugo and Lopez, Karla and Aguilar Vasquez, Mynor and Sandoval, Mario and Lam, Ka On and Cuffe, Sinead and Kelly, Cathy and Geva, Ravit and Hubert, Ayala and Beny, Alex and Brenner, Baruch and Giuseppe, Aprile and Falcone, Alfredo and Maiello, Evaristo and Passalacqua, Rodolfo and Montesarchio, Vincenzo and Hara, Hiroki and Chin, Keisho and Nishina, Tomohiro and Komatsu, Yoshito and Machida, Nozumo and Hironaka, Shuichi and Satoh, Taroh and Tamura, Takao and Sugimoto, Naotaoshi and Cho, Haruhiko and Omuro, Yashushi and Kato, Ken and Goto, Masahiro and Hyodo, Ichinosuke and Yoshida, Kazuhiro and Baba, Hideo and Esaki, Taito and Furuse, Junji and Wan Mohammed, Wan Zamaniah and Hernandez Hernandez, Carlos and Casas Garcia, Juan and Dominguez Andrade, Adriana and Clarke, Katriona and Hjortland, Geir and Glenjen, Nils and Kubiatowski, Tomasz and Jacek, Jassem and Wojtukiewicz, Marek and Lazarev, Sergey and Lancukhay, Yuri and ... and KEYNOTE-061 Investigators and KEYNOTE-061 investigators
The Lancet, ISSN 0140-6736, 07/2018, Volume 392, Issue 10142, pp. 123 - 133
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 02/2012, Volume 90, Issue 2, pp. 331 - 339
Complete congenital stationary night blindness (cCSNB) is a clinically and genetically heterogeneous group of retinal disorders characterized by nonprogressive... 
COMPLETE FORM | LIGHT RESPONSE | CHANNEL | MGLUR6 | SYNAPTIC-TRANSMISSION | MOUSE MODEL | GENETICS & HEREDITY | NYCTALOPIN | RICH REPEAT PROTEIN | MUTATIONS | CONE ELECTRORETINOGRAM | Electroretinography - methods | Night Blindness - metabolism | Humans | Dark Adaptation - genetics | Retinal Rod Photoreceptor Cells - metabolism | Gene Knockdown Techniques - methods | Myopia - metabolism | Receptors, Metabotropic Glutamate - genetics | Retinal Bipolar Cells - physiology | Chromosome Mapping - methods | Genetic Diseases, X-Linked | Night Blindness - genetics | Retinal Bipolar Cells - metabolism | Eye Diseases, Hereditary | Signal Transduction | Mice, Inbred C57BL | Zebrafish | Mice, Inbred C3H | Myopia - genetics | Animals | Myopia - physiopathology | Pedigree | Night Blindness - physiopathology | Retinal Rod Photoreceptor Cells - physiology | Heterozygote | Mice | Receptors, G-Protein-Coupled - genetics | Mutation | Chromosome mapping | Usage | Gene mutations | Retinal bipolar cells | Causes of | Physiological aspects | Night blindness | Genetic aspects | Research | Analysis | Genetic disorders | Animal models | Antibodies | Insertion | stationary night blindness | Retina | Guanine nucleotide-binding protein | Electroretinograms | Depolarization | Signal transduction | Vision | Bipolar cells | Gene mapping | DNA sequencing | Report
Journal Article
Journal of Neurophysiology, ISSN 0022-3077, 11/2012, Volume 108, Issue 9, pp. 2442 - 2451
Journal Article
by Srivastava, A. K and Wang, Y and Huang, R and Skinner, C and Thompson, T and Pollard, L and Wood, T and Luo, F and Stevenson, R and Polimanti, R and Gelernter, J and Lin, X and Lim, I. Y and Wu, Y and Teh, A. L and Chen, L and Aris, I. M and Soh, S. E and Tint, M. T and MacIsaac, J. L and Yap, F and Kwek, K and Saw, S. M and Kobor, M. S and Meaney, M. J and Godfrey, K. M and Chong, Y. S and Holbrook, J. D and Lee, Y. S and Gluckman, P. D and Karnani, N and Kapoor, A and Lee, D and Chakravarti, A and Maercker, C and Graf, F and Boutros, M and Stamoulis, G and Santoni, F and Makrythanasis, P and Letourneau, A and Guipponi, M and Panousis, N and Garieri, M and Ribaux, P and Falconnet, E and Borel, C and Antonarakis, S. E and Kumar, S and Curran, J and Blangero, J and Chatterjee, S and Akiyama, J and Auer, D and Berrios, C and Pennacchio, L and Donti, T. R and Cappuccio, G and Miller, M and Atwal, P and Kennedy, A and Cardon, A and Bacino, C and Emrick, L and Hertecant, J and Baumer, F and Porter, B and Bainbridge, M and Bonnen, P and Graham, B and Sutton, R and Sun, Q and Elsea, S and Hu, Z and Wang, P and Zhu, Y and Zhao, J and Xiong, M and Bennett, David A and Hidalgo-Miranda, A and Romero-Cordoba, S and Rodriguez-Cuevas, S and Rebollar-Vega, R and Tagliabue, E and Iorio, M and D’Ippolito, E and Baroni, S and Kaczkowski, B and Tanaka, Y and Kawaji, H and Sandelin, A and Andersson, R and Itoh, M and Lassmann, T and Hayashizaki, Y and Carninci, P and Forrest, A. R. R and Semple, C. A and Rosenthal, E. A and Shirts, B and ... and The Philippine Cardiogenomics Study Group and Melbourne Genomics Health Alliance and Lifepool and NHLBI GO Exome Sequencing Project and on behalf of 1 and Clark Kendrick C. Go and GUSTO study group and CHARGE and NHLBI Exome Sequence Project Working Groups and ICGC PCAWG Structural Alterations Group and The FANTOM5 Consortium and BioNano Genomics and Global Alliance for Genomics and Health - Regulatory and Ethics Working Group and The FANTOM Consortium
Human genomics, ISSN 1479-7364, 05/2016, Volume 10 Suppl 1, Issue S1, p. 12
Journal Article
Nuclear Inst. and Methods in Physics Research, A, ISSN 0168-9002, 05/2019, Volume 925, Issue C, pp. 133 - 147
A new detection system has been installed at the RIKEN Nishina Center (Japan) to investigate decay properties of very neutron-rich nuclei. The setup consists... 
Analysis methodology | Neutron and beta counters | Beta-delayed neutrons | Background correction | INSTRUMENTS & INSTRUMENTATION | NUCLEAR SCIENCE & TECHNOLOGY | BRANCHING RATIOS | PHYSICS, NUCLEAR | PHYSICS, PARTICLES & FIELDS
Journal Article
Acta Physica Polonica B, ISSN 0587-4254, 03/2018, Volume 49, Issue 3, pp. 417 - 428
An ambitious program to measure decay properties, primarily beta-delayed neutron emission probabilities and half-lives, for a significant number of nuclei near... 
PHYSICS, MULTIDISCIPLINARY | ELEMENTS | IMPACT | ASTRONOMY AND ASTROPHYSICS | NUCLEAR PHYSICS AND RADIATION PHYSICS
Journal Article
Journal of Instrumentation, ISSN 1748-0221, 04/2017, Volume 12, Issue 4, pp. P04006 - P04006
Journal Article